Carbs Flashcards

(33 cards)

1
Q

what is carb RDA?

A

130g/day

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2
Q

what is carb?

A

1C: H2O

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3
Q

which isomer of simple sugars (MS) nutritionally important?

A

D isomer

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4
Q

disaccharides are MS condensed by __ bond

A

glycosidic

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5
Q

homopolysacc of glucose?

A

starch, glycogen

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6
Q

examples of heteropolysaccs?

A

glycosaminoglycans, hemicellulose, pectin, gum

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7
Q

soluble fibre

A

fermented by bacteria in colon (SCFA). delay absorp of glu

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8
Q

insoluble fibre

A

prevent constipation

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9
Q

disacc digestion in:

A

mucosal cells of microvilli/brush border

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10
Q

most abundant complex compound in world, insoluble fibre

A

cellulose

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11
Q

fructose crosses by ___

A

facilitated diffusion

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12
Q

fructose is absorbed faster than ____

A

xylitol and sorbitol

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13
Q

in liver, glucose enters cells by ____ and is insulin _____

A

facilitated diffusion; insulin independent (GLUT2)

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14
Q

in muscle and adipose, glu enters cells by fac. diffusion and is insulin ____

A

dependent (GLUT4)

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15
Q

what is hyperglycemia?

A

blood glu lvl above normal –>doesn’t enter cells, not reabsorbed by kidney

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16
Q

diff between IDDM and NIDDM?

A

first is insulin dependent, other is not (cells resistant, control by diet and hypogly drugs)

17
Q

what is renal threshold for gluc?

A

10mmol/L or 180mg/dL –>idneys no longer reabsorb glu as fast as being filtered

18
Q

what is hypoglycemia?

A

blood glu below normal (hypersecretion of insulin)

19
Q

in fasted states, what are increased?

A

glucagon, glu release by liver/musc/adipose, glucocorticoids from adrenal, gluconeogenesis

20
Q

priority of utilization of absorbed MS?

A

energy–>glycogen–>FA–>PPP

21
Q

what is the embden meyerhof path?

22
Q

PDH needs:

A

thiamine pyrophosphate (TPP)

23
Q

why pyruvate needed to keep TCA cycle running?

A

supply oxaloacetate (in presence of CO2)

24
Q

how many coenzymes and prosthetic groups in PDH?

A

5; 3 (TPP, lipoamide, FAD)

25
what is function of TPP?
decarboxylation of a-ketoacids
26
decarboxylation of pyruvate and oxidation of acetate takes place in:
mito matrix
27
ATP synth takes place in:
mito inner mem
28
what is UDP?
step in glycogenesis (uridine 5' diphosphate)
29
which form of glycogen synthase is more active?
dephosphorylated (target of insulin)
30
three fates of G6P?
glycolysis, liver G6phosphatase (to blood/other tissues), PPP
31
why is PPP necessary?
ribose for synth of DNA/RNA/ATP/GTP, provide NADPH for fa synth and for glutathione reductase rxn
32
tissues with active PPP
adrenal, liver, mammary, testes, RBC, ovary, adipose
33
glutathione composed of :
glutamate, cysteine, glycine